Analog of Haemophilus Hin47 with reduced protease activity

ABSTRACT

An isolated and purified analog of Haemophilus influenzae Hin47 protein has a decreased protease activity which is less than about 10% of that of natural Hin47 protein and preferably substantially the same immunogenic properties as natural Hin47 protein. An isolated an purified nucleic acid molecule encoding the Hin47 analog may be provided in a recombinant plasmid which may be introduced into a cell which is grown to produce the Hin47 analog. Immunogenic compositions comprising the Hin47 analog and the encoding nucleic acid may be formulated as vaccines for in vivo administration to a host, including a human, to confer protection against diseases caused by a bacterial pathogen, including Haemophilus species, such as Haemophilus influenzae, that produces Hin47 protein or a protein capable of inducing antibodies in the host specifically reactive with Hin47 protein. The Hin47 analog and the encoding nucleic acid also may be employed in diagnostic applications.

REFERENCE TO RELATED APPLICATION

This application is is a continuation of U.S. patent application Ser. No. 08/296,149 filed Aug. 26, 1994, which a continuation-in-part of U.S. patent application Ser. No. 08/278,091 filed Jul. 21, 1994, now U.S. Pat. No. 5,506,139.

FIELD OF THE INVENTION

The present invention relates to the field of immunology and is particularly concerned with immunogens and antigens from species of Haemophilus.

BACKGROUND OF THE INVENTION

Haemophilus Influenzae is the organism responsible for a variety of serious human diseases, such as meningitis, epiglotitis, pneumonia and otitis media. Haemophilus influenzae type b (Hib) is a major cause of bacterial meningitis in children under the age of five years. Protective antibodies to the disease are induced by the capsular polysaccharide of the organism and vaccines have been developed that utilise the purified polyribosyl ribitol phosphate (PRP) as the antigen. This vaccine provides 90% protection in adults and in children over 24 months of age, but was ineffective in children under 24 months (Zangwill et al 1993). (The references are identified in a list of references at the end of this disclosure, each of which reference in the list is hereby incorporated by reference without further reference thereto). Like other polysaccharide antigens, PRP does not induce the proliferation of T-helper cells, and reimmunisation fails to elicit either a booster response or an increase in memory cells. Conjugation of the PRP polysaccharide with protein carriers confers T-cell dependent characteristics to the vaccine and substantially enhances the immunologic response to the PRP antigen. Currently, there are four PRP-carrier conjugate vaccines available. These are vaccines based upon H. influenzae type b capsular polysaccharide conjugated to diphtheria toxoid, tetanus toxoid, or Neisseria meningitidis outer membrane protein (reviewed in Zangwill et al, 1993). These H. influenzae b conjugate vaccines have dramatically reduced the incidence of bacterial meningitis (Schoendorf et al, 1994).

There are six serotypes of H. influenzae designated a to f, which are defined by their capsular polysaccharides. The current Haemophilus conjugate vaccines do not protect against other invasive typable strains (types a and c) and, importantly, do not protect against non-typable (NTHi) strains which are a common cause of postpartum and neonatal sepsis, pneumonia and otitis media. Otitis media is the most common illness of early childhood with approximately 70% of all children suffering at least one bout of otitis media before the age of seven. Chronic otitis media can lead to hearing, speech, and cognitive impairment in children. It is caused by bacterial infection with Streptococous pneumoniae (approximately 50%), non-typable H. influenzae (approximately 30%), and Moraxella (Branhamella) catarrhalis (approximately 20%). In the U.S. alone, treatment of otitis media costs between 1 and 2 billion dollars per year for antibiotics and surgical procedures, such as tonsillectomies, adenoidectomies and insertion of tympanostomy tubes. To achieve universal protection against H. influenzae related diseases, particularly in the two to six month age group and certain high risk groups, the provision of conserved, cross-reactive non-capsular H. influenzae immunogens is desirable. Non-typable strains of H. influenzae are also important pathogens responsible for pneumonia in the elderly and other individuals who are particularly susceptible to respiratory infections. There is thus a need for antigens from H. influenzae which are useful as components in immunogenic preparations that provide protection against the many serotypes of H. influenzae. PCT application WO 92/10936, published Jul. 9, 1992 and incorporated herein by reference thereto, describes a 47,000 molecular weight outer membrane protein obtained from H. influenzae that is reported to be an adhesin and has been termed Hin47 that is immunologically conserved between non-typable, type b and non-typed clinical isolates of H. influenzae. The amino acid sequence of Hin47 and the nucleotide sequence of the gene encoding Hin47 were presented at the American Society of Microbiology (ASM) conference held in New Orleans, May 26-30, 1992. These sequences have also been published in PCT application WO 94/00149, published Jan. 6, 1994 and incorporated herein by reference thereto.

Since Hin47 is conserved among strains of Haemophilus influenzae, and is reported to be an adhesin, the protein has utility in diagnosis of and vaccination against disease caused by H. influenzae or other bacterial pathogens that produce Hin47 or a protein capable of raising antibodies specifically reactive with Hin47.

A disadvantage of Hin47 for use as an antigen in diagnosis, for the generation of anti-Hin47 antibodies useful in diagnosis and as an immunogen in vaccination is the unexpected discovery by the present applicants that Hin47 has protease activity which results in the autodigestion of Hin47 and the proteolytic degradation of other antigens mixed therewith.

It would be advantageous to provide analogs of Hin47 protein (sometimes referred to herein as mutants or derivatives) that are substantially reduced in proteolytic activity for use as antigens, immunogenic preparations including vaccines, carriers for other immunogens and the generation of diagnostic reagents.

SUMMARY OF THE INVENTION

The present invention is directed towards the provision of analogs of Haemophilus Hin47 protein having reduced protease activity.

In accordance with one aspect of the invention there is provided an isolated and purified analog of Haemophilus influenzae Hin47 protein having a decreased protease activity which is less than about 10% of natural Hin47 protein. Such Hin47 analog preferably has substantially the same immunogenic properties of natural Hin47 protein. The analog of the present invention may be produced by chemical, biochemical or genetic modification of natural Hin47.

In one embodiment of the present invention, when the analog is produced by genetic modification, at least one amino acid of the natural Hin47 contributing to protease activity may be deleted or replaced by a different amino acid to produce the reduced protease activity. Alternatively, the reduced protease activity may be achieved by inserting at least One amino acid into the natural Hin47 protein. The at least one deleted or replaced amino acid may be selected from amino acids 195 to 201 of Hin47, and specifically may be Serine-197, which may be deleted or replaced by alanine. In addition, the at least one deleted or replaced amino acid may be His-91 and may be deleted or replaced by alanine or lysine or arginine. Further, the at least one deleted or replaced amino acid may be Asp-121 and may be deleted or replaced by alanine or glutamic acid.

In a further aspect, the present invention provides an isolated and purified nucleic acid molecule comprising a mutant Haemophilus influenzae hin47 gene encoding an analog of Haemophilus influenzae Hin47 protein having a reduced protease activity which is less than about 10% of natural Hin47 protein. The mutant hin47 gene may encode any of the Hin47 analogs discussed above. The mutant gene preferably is formed by site-directed mutagenesis of a wild-type hin47 gene. The nucleic acid molecule may be contained in a recombinant plasmid adapted for transformation of a host and may be plasmid DS-1011-1-1 (deposited on Jul. 27, 1994 at American type Culture Collection under Accession No. 75845. The invention also includes a transformed cell containing such a recombinant plasmid.

The present invention, in another aspect, includes a method for producing an analog of Haemophilus influenzae Hin47 protein having a reduced protease activity which is less than about 10% of natural Hin47 protein, which comprises identifying at least one amino acid residue of Hin47 protein which contributes to protease activity thereof, effecting site-directed mutagenesis of the hin47 gene to remove or replace a nucleotide sequence encoding the at least one amino acid and to produce a mutated hin47 gene, introducing the mutated hin47 gene into a cell to produce a transformed cell and growing the transformed cell to produce the Hin47 analog. The at least one amino acid which is selected may be any of the ones specifically identified above with respect to the Hin47 analog.

The introduction of the mutated hin47 gene preferably produces a transformed cell in which the mutated hin47 gene is under control of the T7 promoter and the growing of the transformed cell and expression of the Hin47 analog by the T7 promoter then preferably is effected by culturing in an inducing concentration of lactose. Preferably, the introduction of the mutated hin47 is effected by transforming the cell with the recombinant plasmid DS-1011-1-1, sometimes otherwise referred to as plasmid pT7/Hin47*.

A further aspect of the invention provides a method of providing isolated and purified Hin47 analog, which comprises effecting the procedure described above for the production of the Hin47 analog to produce grown transformed cells harbouring inclusion bodies containing the Hin47 analog, disrupting the grown transformed cells to produce supernatant and the inclusion bodies, solubilizing the inclusion bodies to produce a solution containing Hin47 analog, chromatographically purifying the Hin47 analog from the solution free from cell debris, and isolating the purified Hin47 analog.

The analogs of Hin47 provided herein with their decreased proteolytic activity are useful as antigens in immunogenic composition, carriers for other immunogens, diagnostic agents and in the generation of diagnostic agents. The nucleic acid molecules also are useful as probes for diagnostic use and also as in immunogenic compositions.

In a further aspect of the invention, there is provided an immunogenic composition comprising an immuno-effective amount of the Hin47 analog or of the nucleic acid molecule including the gene encoding the Hin47 analog. The immunogenic composition may be formulated as a vaccine for in vivo administration to a host, including a human, to confer protection against diseases caused by a bacterial pathogen that produces Hin47 or a protein capable of inducing antibodies in the host specifically reactive with Hin47. The bacterial pathogen may be a Haemophilus species, such as Haemophilus influenzae. The immunogenic compositions of the invention may further comprise at least one other immunogenic or immunostimulating material, such as an adjuvant. In an additional embodiment, the nucleic acid molecule comprising a gene encoding the Hin47 analog may be contained within a live vector, such as a pox virus, Salmonella, poliovirus, adenovirus, vaccinia or BCG.

The invention also extends to a method of generating an immune response in a host, including a human, comprising administering thereto an immuno-effective amount of the immunogenic compositions provided herein.

As mentioned above, the Hin47 analog provided herein is useful in diagnostic applications. Accordingly, in an additional aspect of the invention, there is provided a method of determining the presence of antibodies specifically reactive with Hin47 in a sample, comprising the steps of:

(a) contacting the sample with the Hin47 analog having substantially the same immunogenic properties as the natural Hin47 protein as provided herein to produce complexes comprising the Hin47 analog and any such antibodies present in the sample specifically reactive therewith; and

(b) determining production of the complexes.

The present invention also provides a method of determining the presence of Hin47 in a sample, comprising the steps of:

(a) immunizing a subject with an immunogenic composition as provided herein to produce antibodies specific for Hin47 protein;

(b) contacting the sample with the antibodies to produce complexes comprising any Hin47 present in the sample and the Hin47 specific antibodies; and

(c) determining production of the complexes.

The invention also extends to a diagnostic kit for determining the presence of antibodies in a sample specifically reactive with Hin47 , comprising:

(a) the Hin47 analog having substantially the same immunogenic properties as the natural Hin47 protein as provided herein;

(b) means for contacting the analog with the sample to produce a complex comprising the analog and any such antibodies present in the sample; and

(c) means for determining production of the complex.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the restriction maps of plasmids JB-1031-1-14 and JB-1068-2-2 and the construction of the plasmids for sequence analysis;

FIG. 2 shows the full nucleotide (SEQ ID NO: 1) and deduced amino acid sequence (SEQ ID NO: 2) of Hin47 from H. influenzae strain SB33 as well as a partial nucleotide sequence (SEQ ID NO: 3) and a partial deduced amino acid sequence (SEQ ID NO: 4) thereof, the latter being specifically copied by an inventor herein from materials presented in the ASM conference as described above;

FIG. 3 shows a comparison of the amino acid sequences of H. influenzae Hin47 (SEQ ID NO:2), E. coli htrA (SEQ ID NO: 5), and Salmonella typhimurium htrA (SEQ ID NO:6);

FIG. 4 shows an alignment of amino acid residues 57 to 256 of Hin47 with certain known proteases (SEQ ID NOS: 7 to 16). Codes are as follows: TON, rat tonin; PKAAB, kallikrein; PTN, trypsin; CHAA, chymotrypsin; EST, elastase: RP2A, rat mast cell protease; SGT, Streptomyces griseus trypsin; SGBE, S. griseus proteinase A; SGA, S. griseus proteinase B; ALP, L enzymogenes alpha-lyric protease; hin47, res. 57-256 of Hin47. Asterisks(*) denote structurally conserved regions. The catalytic triad residues are indicated by a hash mark (#). `con` refers to regions of structural concensus, among the mammalian proteases;

FIG. 5 shows the restriction maps for plasmids DS-1011-1-1 and DS-1048-2 which express a Hin47 analog from E. coli and a construction scheme for plasmid DS-1011-1-1 (plasmid pT7/Hin47*);

FIG. 6 shows a process for purifying the Hin47 analog from E. coli according to one embodiment of the present invention and gel analysis of the purified product;

FIG. 7 shows the protease activities of natural Hin47 and Hin47 analog towards β-casein;

FIG. 8 shows the stability of natural Hin47 and the Hin47 analog at different temperatures;

FIG. 9 shows the enzymatic degradation of an H. influenzae recombinant protein by natural Hin47 and the Hin47 analog; and

FIG. 10 shows the comparative immunogenicity of natural Hin47 and the Hin47 analog in mice.

GENERAL DESCRIPTION OF INVENTION

Any Haemophilus strains that have Hin47 genes may be conveniently used to provide the purified and isolated nucleic acid molecules (which may be in the form of DNA molecules), comprising at least a portion coding for Hin47 as typified by embodiments of the present invention. Such strains are generally available from clinical sources and from bacterial culture collections, such as the American Type Culture collection. Such strains include H. influenzae strains and other bacteria that produce a protein capable of generating antibodies that specifically recognize Hin47 fragment or analog thereof. Appropriate strains of Haemophilus may include:

H. influenzae type b strain MinnA;

H. influenzae type b strain Eagan;

H. influenzae non-typable strain SB33; or

H. influenzae non-typable strain PAK 12085.

Referring to FIG. 1, there is illustrated restriction maps of plasmids JB-1031-1-14 and JB-1068-2-2 that contain a portion encoding Hin47 protein from non-typable H. influenzae SB33. The nucleotide sequence of the Hin47 gone was determined and is shown in FIG. 2 along with the deduced amino acid sequence of the Hin47 protein. Referring to FIG. 3, there is shown an amino acid sequence alignment of H. influenzae Hin47 and the serine proteases htrA from Escherichia coli and htrA from Salmonella typhimurium. This alignment for the first time reveals the unexpected discovery of the present applicants that Hin47 is related to bacterial serine proteases and that Hin47 has protease activity. Hin47 has previously been reported to be an adhesin. The discovered protease activity thereof greatly limits the usefulness of natural Hin47 as an immunogen for vaccination and as an antigen in diagnostic uses. The sequence alignment shown in FIG. 3 revealed that the htrA proteins and Hin47 contain a GNSGGAL (SEQ ID NO: 17) sequence between residues 195 and 201 of the mature protein. The consensus sequence of the active site of serine proteases is GDSGGPK (SEQ ID NO: 18) (Brenner, 1988) and the active residue is serine. Thus, Serine-197 in Hin47 was mutated to produce an analog of Hin47 reduced in protease activity, in accordance with .one embodiment of the invention. In a particular embodiment, Serine-197 was replaced by alanine. Amino acid residues 57 to 256 of Hin47 were further aligned with known proteases and the active site residues identified from the local homologies surrounding the residues of the catalytic triad (FIG. 4). There is a standard numbering system for serine proteases in which the catalytic triad residues are numbered as His-57, Asp-102 and Ser-195. These correspond to residues His-91, Asp-121 and Ser-197 in the sequential numbering system. Thus, referring to FIG. 4, there is shown a structure-based alignment of ten structurally determined serine proteases (SEQ ID NOS: 7 to 16) in which homologous residues are aligned primarily on the basis of similar locations in three-dimensional space. The location of many .of the residues in the hydrophobic core of Hin47 , as well as residues around the active site can be aligned reasonably well to identify functional amino acids of the Hin47 protease. Thus, other amino acid residues in Hin47 that contribute to protease activity of the protein include His-91 and Asp-121. In particular embodiments, His-91 may be replaced by alanine, lysine or arginine. In an additional embodiment, Asp-121 may be replaced by alanine or glutamic acid. Although the provision of an analog of Hin47 having reduced protease activity has been exemplified herein by particular amino acid substitution within Hin47 protein, the discovery of the protease activity and the methods of Hin47 expression, purification and analysis provided herein, allow for the production of other analogs having at least one other amino acid deleted or replaced or having at least one additional amino acid inserted into the Hin47 protein. In particular applications and embodiments, it may be desirable to simultaneously alter several amino acids of the Hin47 protein to particularly reduce the protease activity of Hin47. Accordingly, the present invention provides analogs of Hin47 protein having decreased protease activity due to single or multiple amino acid deletions, replacements or additions within the Hin47 protein.

Referring to FIG. 5, there is illustrated plasmids DS-1011-1-1 and DS-1048-2 which express a Hin47 analog serine-197 → alanine in E. coli. FIG. 6 shows a flow diagram of a method for the purification of the Hin47 analog from E. coli inclusion bodies.

FIG. 7 shows the reduced protease activity of the Hin47 serine-197 → alanine analog on the substrate β-casein and demonstrates the analog to have less than about 10% of the protease activity of natural Hin47 protein. Thus, in one embodiment of the invention, there is provided an analog of Hin47 having a protease activity of less than about 10% of the protease activity of natural Hin47 and such analog may specifically have amino acid Serine-197 replaced by alanine.

Referring to FIG. 8, there is illustrated an analysis of the increased stability of an analog of Hin47 as provided herein. Thus, in one embodiment of the present invention, there is provided an analog of Hin47 protein having increased thermal stability, and such analog may specifically have amino acid serine-197 replaced by alanine.

Referring to FIG. 9, there is illustrated the proteolytic degradation of a non-Hin47 Haemophilus antigen by Hin47 and a Hin47 analog as provided herein. Thus, in accordance with a further embodiment of the present invention, there is provided an analog of Hin47 compatible with a second non-Hin47 protein and such analog may specifically have amino acid Serine-197 replaced by alanine.

Referring to FIG. 10 and Table 1, there is illustrated the comparative immunogenicity of unmodified Hin47 and a Hin47 analog having reduced protease activity in mice. The Hin47 protein and Hin47 analog had comparable immunogenicity. Thus, in a particular embodiment, there is provided an analog of Hin47 having reduced protease activity and having substantially the same immunogenic properties of natural Hin47 protein. Such analog may specifically have amino acid Serine-197 replaced by alanine.

Referring to Table 2, there is shown the immunoprotective properties of an analog of Hin47 having reduced protease activity against Hib in the infant rat model of bacteraemia, according to an embodiment of the invention and such analog may specifically have amino acid Serine-197 replaced by alanine.

In accordance with another aspect of the present invention, there is provided a vaccine against Haemophilus or other bacterial pathogens that produce Hin47 or a protein capable of inducing antibodies that specifically recognize Hin47, comprising an immunogenically-effective amount of an immunoprotective analog of Hin47 as provided herein or a nucleic acid molecule having a sequence encoding a Hin47 analog as provided herein, and a physiologically-acceptable carrier therefor. The provided analogs also may be used as a carrier protein for hapten, polysaccharides or peptides to make a conjugate vaccine against antigenic determinants unrelated to Hin47.

As will be apparent from the following disclosure, the present invention further provides plasmids and novel strains of bacteria for production of Hin47 analogs as provided herein.

The purified and isolated DNA molecules comprising at least a portion coding for an analog of Haemophilus influenzae Hin47 protein having reduced protease activity compared to natural Hin47 typified by the embodiments described herein, are advantageous as nucleic acid probes for the specific identification of Haemophilus strains in vitro or in vivo. The Hin47 analogs encoded by the DNA molecules provided herein are useful as diagnostic reagents as antigens or for the generation of anti-Hin47 antibodies, antigens for the vaccination against the diseases caused by species of Haaemophilus and other bacterial pathogens that produce a protein capable of producing antibodies that specifically recognise Hin47 and for detecting infection by Haemophilus and other such bacteria.

In additional embodiments of the present invention, the Hin47 analogs having reduced protease activity as provided herein may be used as carrier molecules to prepare chimetic molecules and conjugate vaccines (including glycoconjugates) against pathogenic bacteria, including encapsulated bacteria. Thus, for example, glycoconjugates of the present inventions may be applied to vaccinations to confer protection against disease and infection caused by any bacteria having polysaccharide antigens including lipooligosaccharides (LOS) and PRP. Bacterial pathogens may include; for example, Haemophilus influenzae, Streptococcus pneumoniae, Escherichia coli, Neisseria meningitidis, Salmonella typhi, Streptococcus mutans, Cryptococcus neoformans, Klebsiella, Staphylococcus aureus and Pseudomonas aeruginosa. Particular antigens which can be conjugated to analogs of Hin47 and methods to achieve such conjugations are described in applicants published PCT application WO 94/12641 which is hereby incorporated by reference thereto.

In another embodiment, the carrier function of Hin47 analogs may be used, for example, to induce immunity toward abnormal polysaccharides of tumor cells, or to produce anti-tumor antibodies that can be conjugated to chemotherapeutic or bioactive agents.

Accordingly, the present invention provides the primary sequence and the preparation of an analog of Hin47 of H. influenzae that can be used in the prevention and diagnosis of diseases caused by H. influenzae. In particular, the inventors discovered that the Hin47 analog can elicit protective immune responses against live H influenzae type b bacterial challenge. Thus, the present inventions have utility in vaccines. The invention also discloses the nucleotide sequences of the gene encoding the Hin47 analog. These DNA segments may be used to provide an immunogen essentially free from other H influenzae antigens,. such as PRP and lipooligosaccharides (LOS), through the application of recombinant DNA technology. The Hin47 analog protein, may be produced in a suitable expression system, such as E. coli, Haemophilus, Bacillus, Bordetella Fungi, Yeast, Baculovirus, Poxvirus, vaccinia or mammalian expression systems. The present disclosure further provides novel techniques which can be employed for preparing essentially pure Hin47 analogs.

It is clearly apparent to one skilled in the art, that the various embodiments of the present invention have many applications in the fields of vaccination, diagnosis, treatment of, for example, Haemophilus infections, and infections with other bacterial pathogens that produce proteins capable of producing antibodies that specifically recognize Hin47 and the generation of immunological reagents. A further non-limiting discussion of such uses is further presented below.

1. Vaccine Preparation and Use

Immunogenic compositions, suitable to be used as vaccines, may be prepared from Hin47 analogs as disclosed herein. The vaccine elicits an immune response in a subject which produces antibodies, including anti-Hin47 antibodies and antibodies that are opsonizing or bactericidal. Should the vaccinated subject be challenged by Haemophilus or other bacteria that produce proteins capable of producing antibodies that specifically recognize Hin47 , the antibodies bind to and inactivate the bacterium. Furthermore, opsonizing or bactericidal anti-Hin47 antibodies may also provide protection by alternative mechanisms.

Immunogenic compositions including vaccines may be prepared as injectables, as liquid solutions or emulsions. The Hin47 analogs may be mixed with pharmaceutically acceptable excipients which are compatible with the Hin47 analog. Such excipients may include, water, saline, dextrose, glycerol, ethanol, and combinations thereof. The immunogenic compositions and vaccines may further contain auxiliary substances, such as wetting or emulsifying agents; pH buffering agents, or adjuvants to enhance the effectiveness thereof. Methods of achieving adjuvant effect include the use of agents such as aluminumhydroxide or phosphate (alum), commonly used as 0.05 to 0.1 percent solution in phosphate buffered saline. Immunogenic compositions and vaccines may be administered parenterally, by injection subcutaneously or intramuscularlyl Alternatively, the immunogenic compositions formed according to the present invention, may be formulated and delivered in a manner to evoke an immune response at mucosal surfaces. Thus, the immunogenic composition may be administered to mucosal surfaces by, for example, the nasal or oral (intragastric) routes. Alternatively, other modes of administration including suppositories and oral formulations may be desirable. For suppositories, binders and carriers may include, for example, polyalkalene glycols or triglycerides. Oral formulations may include normally employed incipients such as, for example, pharmaceutical grades of saccharine, cellulose and magnesium carbonate. These compositions can take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations or powders and contain about 1 to 95% of the Hin47 analogs. The immunogenic preparations and vaccines are administered in a manner compatible with the dosage formulation, and in such amount as will be therapeutically effective, protective and immunogenic. The quantity to be administered depends on the subject to be treated, including, for example, the capacity of the individual's immune system to synthesize antibodies, and if needed, to produce a cell-mediated immune response. Precise amounts of active ingredient required to be administered depend on the judgment of the practitioner. However, suitable dosage ranges are readily determinable by one skilled in the art and may be of the order of micrograms of the Hin47 analogs. Suitable regimes for initial administration and booster doses are also variable, but may include an initial administration followed by subsequent administrations. The dosage may also depend on the route of administration and will vary according to the size of the host.

The concentration of antigen in an immunogenic composition according to the invention is in general about 1 to 95%. A vaccine which contains antigenic material of only one pathogen is a monovalent vaccine. Vaccines which contain antigenic material of several pathogens are combined vaccines and also belong to the present invention. Such combined vaccines contain, for example, material from various pathogens or from various strains of the same pathogen, or from combinations of various pathogens.

The nucleic acid molecules encoding the Hin47 analog of the present invention may also be used directly for immunization by administration of the DNA directly, for example, by injection for genetic immunization or by constructing a live vector, such as Salmonella, BCG, adenovirus, poxvirus, vaccinia or poliovirus. A discussion of some live vectors that have been used to carry heterologous antigens to the immune system are discussed in, for-example, O'Hagan (1992). Processes for the direct injection of DNA into test subjects for genetic immunization are described in, for example, Ulmer et al, 1993.

2. Immunoassays

The Hin47 analogs of the present invention are useful as immunogens for the generation of anti-Hin47 antibodies, as antigens in immunoassays, including enzyme-linked immunosorbent assays (ELISA), RIAs and other non-enzyme linked antibody binding assays or procedures known in the art for the detection of anti-bacterial, Haemophilus, and anti-Hin47 antibodies. In ELISA assays, the Hin47 analogs, are immobilized onto a selected surface, for example, a surface capable of binding proteins such as the wells of a polystyrene microtiter plate. After washing to remove incompletely adsorbed Hin47 analogs, a nonspecific protein such as a solution of bovine serum albumin (BSA) that is known to be antigenically neutral with regard to the test sample may be bound to the selected surface. This allows for blocking of nonspecific adsorption sites on the immobilizing surface and thus reduces the background caused by nonspecific bindings of antisera onto the surface.

The immobilizing surface is then contacted with a sample, such as clinical or biological materials, to be tested in a manner conducive to immune complex (antigen/antibody) formation. This may include diluting the sample with diluents, such as solutions of BSA, bovine gamma globulin (BGG) and/or phosphate buffered saline (PBS)/Tween. The sample is then allowed to incubate for from 2 to 4 hours, at temperatures such as of the order of about 25° to 37° C. Following incubation, the sample-contacted surface is washed to remove non-immunocomplexed material. The washing procedure may include washing with a solution, such as PBS/Tween or a borate buffer. Following formation of specific immunocomplexes between the test sample and the bound Hin47 analogs, and subsequent washing, the occurrence, and even amount, of immunocomplex formation may be determined by subjecting the immunocomplex to a second antibody having specificity for the first antibody. If the test sample is of human origin, the second antibody is an antibody having specificity for human immunoglobulins and in general IgG. To provide detecting means, the second antibody may have an associated activity such as an enzymatic activity that will generate, for example, a colour development upon incubating with an appropriate chromogenic substrate. Quantification may then be achieved by measuring the degree of colour generation using, for example, a visible spectra spectrophotometer.

3. Use of Sequences as Hybridization Probes

The nucleic acid molecules of the present invention, having the sequence of the hin47 analog gene, allow for the identification and cloning of the Hin47 genes from any species of Haemophilus and other bacteria that produce proteins capable of producing antibodies that specifically recognize Hin47.

The nucleic acid molecules having the sequence encoding the Hin47 analog of the present invention are useful for their ability to selectively form duplex molecules with complementary stretches of other hin47 genes. Depending on the application, a variety of hybridization conditions may be employed to achieve varying degrees of selectivity of the probe toward the other hin47 genes. For a high degree of selectivity, relatively stringent conditions are used to form the duplexes, such as low salt and/or high temperature conditions, such as provided by 0.02M to 0.15M NaCl at temperatures of between about 50° to 70° C. For some applications, less stringent hybridization conditions are required, such as 0.15M to 0.9M salt, at temperatures ranging from between about 20° C. to 55° C. Hybridization conditions can also be rendered more stringent by the addition of increasing amounts of formamide, to destabilize the hybrid duplex. Thus, particular hybridization conditions can be readily manipulated, and will generally be a method of choice depending on the desired results.

In a clinical diagnostic embodiment, the nucleic acid molecules encoding the hin47 genes of the present invention may be used in combination with an appropriate means, such as a label, for determining hybridization. A wide variety of appropriate indicator means are known in the art, including radioactive, enzymatic or other ligands, such as avidin/biotin, which are capable of providing a detectable signal. In some diagnostic embodiments, an enzyme tag, such as urease, alkaline phosphatase or peroxidase, instead of a radioactive tag may be used. In the case of enzyme tags, colorimetric indicator substrates are known which can be employed to provide a means visible to the human eye or spectrophotometrically, to identify specific hybridization with samples containing hin47 gene sequences.

The nucleic acid molecules comprising hin47 genes of the present invention are useful as hybridization probes in solution hybridizations and in embodiments employing solid-phase procedures. In embodiments involving solid-phase procedures, the test DNA (or RNA) from samples, such as clinical samples, including exudates, body fluids (e.g., serum, amniotic fluid, middle ear effusion, sputum, bronchoalveolar lavage fluid) or even tissues, is adsorbed or otherwise affixed to a selected matrix or surface. The fixed, single-stranded nucleic acid is then subjected to specific hybridization with selected probes comprising the nucleic acid sequences of the hin47 genes of the present invention under desired conditions. The selected conditions will depend on the particular circumstances based on the particular criteria required depending on, for example, the G+C contents, type of target nucleic acid, source of nucleic acid, size of hybridization probe etc. Following washing of the hybridization surface so as to remove non-specifically bound probe molecules, specific hybridization is detected, or even quantified, by means of the label.

4. Expression of the Genes Encoding Analogs of Hin47 Having Reduced Protease Activity

Vectors perhaps containing replicon and control sequences which are derived from species compatible with the host cell may be used for the expression of the Hin47 analog genes as provided herein in expression systems. The vector ordinarily carries a replication site, as well as marking sequences which are capable of providing phenotypic selection in transformed cells. For example, E. coli may be transformed using pBR322 which contains genes for ampicillin and tetracycline resistance and thus provides easy means for identifying transformed cells. The pBR322 plasmid, or other microbial plasmid or phage must also contain, or be modified to contain, promoters which can be used by the host cell for expression of its own proteins.

In addition, phage vectors containing replicon and control sequences that are compatible with the host can be used as a transforming vector in connection with these hosts. For example, the phage in lambda GEM™-11 may be utilized in making recombinant phage vectors which can be used to transform host cells, such as E. coli LE392.

Promoters commonly used in recombinant DNA construction include the β-lactamase (penicillinase) and lactose promoter systems (Chang et al, 1979; Goeddel et al, 1980) and other microbial promoters, such as the T7 promoter system (U.S. Pat. No. 4,952,496). Details concerning the nucleotide sequences of promoters are known, enabling a skilled worker to ligate them functionally with plasmid vectors. The particular promoter used will generally be a matter of choice depending upon the desired results. Hosts that are appropriate for expression of the Hin47 analogs include E. coli, Bacillus species, Haemophilus Bordetella fungi, yeast, mammalian cells or the baculovirus expression system may be used.

Thus, in accordance with the invention, it may be preferred to make the Hin47 analog protein by recombinant methods. Particularly desirable hosts for expression in this regard include Gram positive bacteria which do not have LPS and are therefore endotoxin free. Such hosts include species of Bacillus and may be particularly useful for the production of non-pyrogenic Hin47 analog.

Biological Deposits

Plasmid DS-1011-1-1 (pT7/Hin47*) that contains a portion coding for a Hin47 analog that is described and referred to herein has been deposited with the American Type Culture Collection (ATCC) located at Rockville, Md., USA, pursuant to the Budapest Treaty and prior to the filing of this continuation-in-part application on Jul. 27, 1994 under Accession No. 75845. Samples of the deposited plasmids will become available to the public upon grant of a patent based upon this U.S. patent application. The invention described and claimed herein is not to be limited in scope by plasmid deposited, since the deposited embodiment is intended only as an illustration of the invention. Any equivalent or similar plasmids that encode similar or equivalent antigens as described in this application are within the scope of the invention.

EXAMPLES

The above disclosure generally describes the present invention. A more complete understanding can be obtained by reference to the following specific Examples. These Examples are described solely for purposes of illustration and are not intended to limit the scope of the invention. Changes in form and substitution of equivalents are contemplated as circumstances may suggest or render expedient. Although specific terms have been employed herein, such terms are intended in a descriptive sense and not for purposes of limitations.

Methods of molecular genetics, protein biochemistry, and immunology used but not explicitly described in this disclosure and these Examples are amply reported in the scientific literature and are well within the ability of those skilled in the art.

Example 1

This Example illustrates the cloning of the hin47 gene from non-typable H. influenzae strain SB33.

Chromosomal DNA was prepared from H. influenzae strain SB33, and an EMBL3 library was prepared and screened with a labelled oligonucleotide probe specific for the 5'-end of hin47. Non-typable H. influenzae strain SB33 was grown on Mueller-Hinton agar or in brain heart infusion broth as described by Harkhess et al, 1992. Chromosomal DNA was prepared as follows: cells from 50 ml of culture were pelleted by centrifugation at 5000 rpm for 15 to 20 min, at 4° C., in a Sorvall RC-3B centrifuge. The cell pellet was resuspended in 10 ml of TE, (10 mM Tris/HCl, 1 mM EDTA, pH 7.5), pronase was added to 500 μg ml⁻¹ and SDS to 1%. The sample was incubated at 37° C. until a clear lysate was obtained. The lysate was gently extracted once with Tris-saturated phenol (pH 7.4), once with Tris-saturated phenol/chloroform (1:1) and once with chloroform. The final aqueous phase was dialysed at 4° C. for 24 h against 1M NaCl, followed by 24 h against TE.

An EMBL3 library was prepared by partial digestion of SB33 chromosomal DNA with Sau3A I, followed by size fractionation either on a 10 to 30% sucrose gradient in TNE (20 mM Tris/HCl, 5 mM NaCl, 1 mM EDTA, pH 8.0) or by preparative gel electrophoresis. Fractions containing DNA fragments greater than 5 kb in length were pooled, precipitated and ligated with BamH I arms of EMBL3 (Promega). The ligation mixture was packaged using a Gigapack II packaging kit and plated onto E. coli LE392 cells. The libraries were amplified and stored at 4° C. in the presence of 0.3% chloroform.

Plaques were lifted onto nitrocellulose filters for hybridization with a ³² p-labelled oligonucleotide probe (3026.SL). The oligonucleotide sequence was ATGAAAAAAACACGTTTTGTATTAAATAGTATTGCACTTGG (SEQ ID NO: 3) corresponding to the N-terminal amino acid sequence MKKTRFVLNSIALG (SEQ ID NO: 19). Phage DNA was prepared from putative plaques and the insert DNA was excised by Sal I digestion and cloned into pUC8-BgXb digested with Sal I. Plasmids JB-1031-1-14 and JB-1068-2-2 (FIG. 1) were selected for further analysis.

Example 2

This Example illustrates the characterization and sequence analysis of the hin47 gene and deduced amino acid sequence of the Hin47 protein from NTHi strain SB33.

Restriction mapping and Southern blot analysis of clones JB-1031-1-14 and JB-1068-2-2 localized the hin47 gene on a 4.7 kb BamH I/BamH I or a 2.7 kb BamH I/Pst I DNA fragment. The 4.7 kb BamH I/BamH I fragment from JB-1068-2-2 was subcloned into pUCS/BgXb generating plasmid DS-755-1. The 3.1 kb BamH I to Xba I fragment of DS-7551 was subcloned into pUC18 generating plasmid JB-1165-1 which has restriction sites suitable for the Erase-a-base (Promega) procedure (FIG. 1). This technique generates successive clones with increasing truncations of insert DNA, with the deletions occurring from the same end. The resultant nested set of clones can be sequenced rapidly using a universal primer.

DNA from plasmid JB-1165-1 was digested with BamH I and Sao I and subjected to exoIII digestion using an Erase-a-base kit. The resultant set of truncated plasmids was analysed by agarose gel electrophoresis and representative plasmids were selected for sequence analysis.

Plasmid DNA for sequencing wag prepared by a modification of the procedure of Holmes and Quigley, 1981. Briefly, the cell pellet from 50 ml of culture was resuspended in 10 ml STET (8% sucrose, 5% Triton X-100, 50 mM EDTA, and 50 mM Tris/HCl; pH 8.0), lysozyme (2.5 mg) was added and the mixture was boiled for 2 min. The sample was spun at 14,000 rpm. in a Sorvall RC 5B for 20 minutes and the supernatant was precipitated with an equal volume of isopropanol, washed with 70% ethanol then absolute ethanol, and then air dried. The pellet was resuspended in 0.9 ml of TE, then 20 μl of 5 mg ml⁻¹ RNAse A were added, and the mixture was incubated at 37° C. for 15 min. After the addition of 500 μl of 1.5M NaCl/30% PEG, the mixture was incubated on ice for 30 min and the DNA was pelleted by centrifugation in an Eppendorf microfuge for 10 min. The pellet was resuspended in 400 μl of TE and extracted twice with Tris-saturated phenol (pH 7.4), twice with Tris-saturated phenol/chloroform (1:1) and twice with chloroform. The DNA was precipitated by adding 40 μl of 3M ammonium acetate and 1 ml of ethanol, washed with 70% ethanol and resuspended in distilled water.

DNA samples were sequenced using the ABI model 370A DNA sequencer and the dye terminator chemistry. The universal reverse primer was used with the nested set of clones to determine the sequence of the hin47 coding strand. Oligonucleotide primers of approximately 25 bases in length were used to confirm the sequence of the non-coding strand. The nucleotide sequence of the SB33 hin47 gene and the deduced amino acid sequence of the Hin47 protein are shown in FIG. 2. The nucleotide and N-terminal amino acid sequences of Hin47 presented at the ASM meeting, New Orleans, May 26 to 30, 1992 are indicated in lower case on FIG. 2. The amino terminal sequences of the SB33 Hin47 and this presented sequence are identical, establishing the identity of the cloned gene as hin47.

Example 3

This Example describes the discovery of serine protease activity of Hin47 protein. The deduced amino acid sequence of Hin47 protein determined in Example 2 above was compared with all other known proteins in the Genbank data base. As described above Hin47 protein is described in published PCT applications WO 94/00149, WO 92/11367 and WO 92/10936 to be an adhesin molecule of Haemophilus. It was, therefore, a surprising and unexpected discovery of the present invention that Hin47 protein has significant amino acid homology (55%) with the serine proteases E. coli htrA and S. typhimurium htrA and other proteases. These amino acid sequence homologies are shown in FIGS. 3 and 4. Furthermore, Hin47 protein was found to autodigest unless it was stored in the presence of a serine protease inhibitor, such as Pefablock.

Example 4

This Example illustrates the generation of the mutant hin47 gene by site-directed mutagenesis.

As explained above, H. influenzae Hin 47, E. coli htrA, and S. typhimurium htrA are all serine proteases. The consensus sequence of the active site of setins proteases is GDSGGPK (SEQ ID NO: 18) [Brenner, 1988] with serine being the active residue. The htrA proteins both have a GNSGGAL (SEQ ID NO: 17) sequence and in H. influenzae Hin47, there is the identical sequence between residues 195 and 201 of the mature protein. Thus, the serine residue at position 197 was selected for site-directed mutagenesis, to produce an analog of Hin47 with reduced protease activity.

An oligonucleotide CGCTCCACCAGCATTACCGCGG (SEQ ID NO: 20) was synthesized which would change the serine residue at 197 to an alanins. The hin47 gene was cloned into M13mp18 generating clone DS-981-3 and mutagenesis was performed using the Amersham In Vitro Site-Directed Mutagenesis kit. Clone DS-991-8 was confirmed by sequence analysis to contain the mutation Serine-197 to Alanine. This mutant hin47 gene is designated hin47*.

In addition a comparison of the amino acid sequence of Hin47 with other proteases (as shown in FIG. 4) revealed that amino acids His-91 and Asp-121 are sites appropriate for mutagenesis to produce an analog of Hin47 with reduced protease activity. By mutagenesis methods analogous to those described above, HIST91 and/or Asp-121 are deleted or replaced by different amino acids. Such amino acid replacements may include His-91 to Alanine and Asp-121 to Alanins. Olignonucleotides to effect such mutagenesis include:

His-91→Ala-91 5' ATCAATAACAGCATTATTGGT 3' (SEQ ID NO: 21)

Asp-121 →Ala-121 5' TAATGCAATTGCTGATAGTTC3' (SEQ ID NO: 22)

Many serine proteases are'secreted in an inactive (`zymogen`) form, and require clipping to expose their active sites. N terminal sequence analysis of mature natural Hin47 protein suggested the cleavage of the preprotein to occur at KFFFG DRFAEQ (SEQ ID NO: 23). Modifications of amino acids that prevent cleavage of the molecule to produce the active protease molecule can produce an analog of Hin47 having reduced protease activity.

Example 5

This Example illustrates the construction of plasmids expressing Hin47 Set-197 →alanine analog from E. coli.

The mutated hin47* gene from plasmid DS-991-8 was cloned into the pT7-7 expression vector to generate plasmid DS-1011-1-1 (FIG. 5). E. Coli strain BL21/DE3 was transformed to generate E. coli strain DS-1018-3-1 which expresses Hin47 Ser-197 alanine analog upon induction.

In order to utilize tetracycline selection, the hin47, gene was cloned into pBR328. The Bgl II/Cla I T7/hin47*, gene fragment from DS-1011-1-1 was cloned into pEVvrf1 (Young and Davis, 1985) in order to generate a Bg1 II/BamH I fragment which could be cloned into pUC-4K (Pharmacia) digested with Ban I. The resultant clone DS-1034-3 was digested with EcoR I and the T7/hin47* gene fragment cloned into pBR328 (Boehringer Mannheim Corporation) to generate plasmids DS-1048-2 and DS-1067-2. Electroporation of plasmid DNA into E. coli strain BL21/DE3 resulted in strains DS-1071-1-1 and DS-1071-3-1 which express the Hin47 Ser-197 → alanine analog.

Example 6

This Example illustrates the expression of Hin47 Ser-197 → alanine analog from E. coli.

An overnight culture of strains DS-1018-3-1, DS-1071-1-1, or DS-1071-3-1 were grown overnight in NZCYM media+3% dextrose+antibiotics (ampicillin at 25 μg ml⁻¹ or tetracycline at 10 g ml⁻¹), at 37° C., with shaking. A 1:40 dilution of the overnight culture was inoculated into the same medium and grown at 37° C. with shaking until the absorbance was A₅₇₈ approximately 0.3. A 1/10 volume of 10% lactose was then added to induce expression from the T7 promoter. Cell samples were harvested about 4 hours after induction by centrifuging culture samples at 5000 rpm for 10 min in a Sorvall RC-3B, at 4° C.

Example 7

This Example illustrates the extraction and purification of Hin47.

Hin47 was expressed as soluble protein in E. coli. The cell pellet from a 250 ml culture, prepared as described in Example 6, was resuspended in 40 ml of 50 mM Tris-HCl, pH 8.0, and disrupted by sonication (3×10 min, 70% duty circle). The extract was centrifuged at 20,000 ×g and the resulting supernatant which contained >95% of the soluble Hin47 protein was retained. This fraction was called "Hin47-extract".

This Hin47-extract was further purified on a DEAE Sephacel column. Forty ml of the Hin47-extract was applied onto a 20-ml DEAE Sephacel column equilibrated in 50 mM Tris-HCl, pH 8.0. Hin47 bound to the column under these conditions. The column was washed with 100 ml of 50 mM Tris-HCl, pH 8.0, and then washed with 100 ml of 50 mM Tris-HCl, pH 8.0 containing 20 mM NaCl. Hin47 was then eluted with 50 mM Tris-HCl, pH 8.0, containing 40 mM NaCl. The amount of Hin47 in the fractions was determined by the BCA protein assay. The purity of Hin47 was assessed by SDS-PAGE analysis. The fractions containing Hin47 were combined and stored at -20° C.

Example 8

This Example illustrates the extraction and purification of Hin47 Set-197 → alanine analog.

Hin47 Ser-197 → alanine analog was expressed in inclusion bodies in E. coli. The cell pellet from a 250 ml culture, prepared as described in Example 6, was resuspended in 40 ml of 50 mM Tris-HCl, pH 8.0, and disrupted by sonication (3×10 min, 70% duty circle). The extract was centrifuged at 20,000 ×g and the resulting pellet was saved. The pellet was re-extracted with 40 ml of 50 mM Tris-HCl, 0.5% Triton X-100, 10 mM EDTA, pH 8.0. The suspension was sonicated 10 min at 70% duty circle. The extract was centrifuged at 300 ×g for 5 min. The resultant supernatant was centrifuged again at 20,000 ×g for 30 min and the resultant-pellet was saved. The pellet was resuspended in 50 mM Tris-HCl, 0.5% Triton X-100, 10 mM EDTA, pH 8.0. The suspension was then mixed with 50 mM Tris-HCl, pH 8.0 Containing 8M urea. The final urea concentration in the mixture was adjusted to 2M with 50 mM Tris-HCl, pH 8.0. Hin47 Ser-197 → alanine analog was completely solubilized under these conditions. The final volume of the solution was 20 ml. This fraction is called "Hin47 analog-extract". The Hin47 analog-extract was further purified on a DEAE Sephacel column. Twenty ml of Hin47 analog-extract was applied onto a 10 ml DEAE Sephacel column equilibrated in 50 mM Tris-HCl, pH 8.0. Hin47 Ser-197 → alanine analog bound to the column under these conditions. The column was washed with 50 mM Tris-HCl, pH 8.0, and Hin47 analog was eluted with 50 mM Tris-HCl, pH 8.0, containing 30, mM NaCl. The amount of Hin47 analog in the fractions was determined by the BCA protein assay. The purity of Hin47 analog was assessed by SDS-PAGE analysis (FIG. 6). The fractions containing Hin47 analog were combined and stored at -20° C.

Example 9

This Example illustrates the protease activity of Hin47 and Hin47 Ser-197 → alanine analog. The enzymatic activity of Hin47 and Hin47 Ser-197 → alanine analog was analyzed using β-casein as a substrate (FIG. 7). The reaction mixtures contained 5 μg of β-casein and either Hin47 or Hin47 analog. The reaction was carried out at 37° C. for two hours, and then stopped by adding the SDS-sample buffer and instantly heating the sample at 100° C. for 5 min. The aliquots were analyzed by SDS-PAGE. As shown in FIG. 7, digestion of β-casein by Hin47 was more obvious after two hours (panel A, lane 1) in comparison to the fractions containing Hin47 analog (panel A, lane 2) or without any exogenous proteins (panel A, lane 3). The presence of Hin47 or Hin47 analog in these mixtures were confirmed by immuno-blotting using a monoclonal antibody to Hin47 (FIG. 7, panel C, lanes 1 and 2).

The protease activities of Hin47 and Hin47 Ser-197 → alanine analog were also compared by analyzing the autodigestion of Hin47 or Hin47 analog at 4° C. and -20° C. The purified Hin47 or analog were stored at either 4° C. or -20° C. for up to 20 days. Allquots were taken on days 0, 10 and 20 and the stability of Hin47 or analog was analyzed by immuno-blotting using a Hin47 monoclonal antibody (FIG. 8). The analog was much more stable than Hin47 up to 20 days when stored at either 4° C. or -20° C.

To further examine the protease activity of the Hin47 Ser-197 → alanine analog, the ability of Hin47 or analog to degrade an 80-kDa H. influenzae recombinant antigen was examined. Thus, a mixed antigen study was performed to determine the proteolytic effect of Hin47 or Hin47 analog on another antigen. An 80 kDa H. influenzae recombinant protein (TBP1) was chosen for this study in order to distinguish it from the Hin47 or analog protein (47 kDa). Five mixtures were formulated as follows: 80 kDa protein alone; 80-kDa protein+Hin47; 80-kDa protein+analog; Hin47 alone; and analog alone. The amount of each protein in the mixture was 5 μg. The mixtures were stored at 4° C. up to four weeks. Aliquots were taken on days 0, 7, 14 and 28 for analysis by SDS-PAGE (FIG. 9). Both the 80 kDa protein and Hin47 were largely degraded after one week (lanes 2 and 4). In contrast, the 80 kDa protein in combination with Hin47 analog remained intact after one week, and showed only slight degradation even after four weeks (lane 3).

Example 10

This Example illustrates the comparative immunogenicity of Hin47 and Hin47 analog in mice. The results of a study to determine the comparative immunogenicity of Hin47 and the Hin47 Ser-197 → alanine analog are shown in FIG. 10. Thus, groups of five Balb/c mice were injected three times (as indicated by arrows) s.c. on days 1, 29 and 43 with 1-μg dose of either Hin47 or Hin47 analog in the presence of AlPO₄ (1.5 mg per dose). Blood samples were taken on days 14, 28, 42 and 56 (as indicated by bleeds 1, 2, 3 and 4, respectively) for analyzing the anti-Hin47 antibody titers by EIAs. The determination of anti-Hin47 antibodies in mouse sera was performed as described by Panezutti et al. (1993). Microtiter wells were coated with 1 μg of either Hin47 or analog for 16 hours at room temperature. The plates were then blocked with 0.1% (w/v) bovine serum albumin in PBS. The mouse sera were serially diluted, added to the wells, then incubated for one hour at room temperature. Affinity-purified F(ab')₂ fragments of goat anti-mouse IgG (Fc specific) antibody conjugated to horseradish peroxidase were used as the second antibody. The reactions were developed using tetramethylbenzidine (TMB/H₂ O₂) and absorbencies were measured at 450 nm (using 540 nm as a reference wavelength) in a Flow Multiskan MCC microplate reader. The reactive titer of an antiserum was defined as the reciprocal of the dilution Consistently showing a two-fold increase in absorbance over that obtained with the pre-bleed serum sample. As can be seen from FIG. 10, both Hin47 and the Hin47 analog elicited comparable IgG titers in mice regardless of whether Hin47 or mutant was used as an antigen in EIAs.

To further examine the immune response to Hin47 or the Hin47 Ser-197 → alanine analog, the subclasses of anti-Hin47 IgG in mouse sera were determined. Microtiter wells were coated with 1 μg of purified Hin47 or analog. The final bleed of mouse serum samples from the comparative immunogenicity study (as described above) were pooled and tested in EIAs. Rat anti-mouse IgG₁, IgG₂₈, IgG_(2b) antibodies conjugated horseradish peroxidase and rabbit anti-mouse IgG₃ conjugated to horseradish peroxidase were used as reagents in EIAs. The working dilution of each conjugate was determined using purified antibody subclasses to avoid cross reactivity. The reactive titers were determined as described above. As shown in Table 1 below, the IgG-subclass profile induced in mice by either Hin47 or Hin47 analog were identical, regardless of whether Hin47 or analog was used as a solid antigen in the EIAs. The predominant IgG response in both groups of mouse sera was of the IgG₁ isotype. Hence, the Hin47 analog exhibited substantially the same immunogenic properties as the natural protein.

Example 11

This Example illustrates the immunoprotective properties of Hin47 and Hin47 Ser-197 → alanine analog.

The immunoprotective properties of Hin47 and the Hin47 Ser-197 → alanine analog were analyzed by the ability of Hin47 specific antisera to protect infant rats against H. Influenzae type b strain MinnA in a bacteremia model. The results of this study are shown in Table 2 below. Groups of nine 6-day old Wistar infant rats were inoculated subcutaneously (s.c.) on the dorsum close to the neck with 0.1 mL of either a rabbit anti-Hin47 analog antiserum or the corresponding prebleed serum. Twenty-four hours later, the animals were challenged intraperitoneally (i.p.) with 700 cfu. of freshly grown Hib Strain MinnA. Blood samples were collected 20 hours post-challenge and plated onto chocolate agar plates. Bacterial colonies were counted after 24 hours. As shown in Table 2, threw out of nine animals in the group inoculated with anti-Hin47 analog antiserum did not show any bacteremia in their blood. Only one mouse in the group inoculated-with anti-Hin47 analog antiserum (11%) had a higher bacteria recovery from the blood sample compared to mice inoculated with prebleed serum. In contrast, bacteria were recovered from all the nine mice inoculated with pre-bleed serum. Four out of nine animals (44%) in the group inoculated with pre-bleed serum showed high levels (500 to 1,000) of bacteria recovered in blood samples.

SUMMARY OF DISCLOSURE

In summary of this disclosure, the present invention provides a novel analog of Haemophilus influenzae Hin47 protein which has a decreased protease activity of less than about 10% of that of the natural Hin47 protein as well as isolated and purified DNA molecules encoding the same.

                  TABLE 1                                                          ______________________________________                                         Hin47 IgG titers in mouse immune sera                                                 IgG titers in Group #1*                                                                      IgG titers in Group #2*                                   IgG Suclass                                                                             To Hin47  To Mutant To Hin47                                                                               To Mutant                                 ______________________________________                                         IgG (H + L)                                                                             102,400   102,400   102,400 102,400                                   IgG.sub.1                                                                               25,600    25,600    25,600  25,600                                    IgG.sub.2a                                                                              <100      <100      <100    <100                                      IgG.sub.2b                                                                              400       400       400     400                                       IgG.sub.3                                                                               <100      <100      <100    <100                                      ______________________________________                                          *Group #1: Immune sera were pooled from a group of five mice received          Hin47 immunization. Group #2: Immune sera were pooled from a group of fiv      mice received Hin47 mutant immunization.                                       Plates were coated with either Hin47 or mutant protein.                  

                  TABLE 2                                                          ______________________________________                                         Protective ability of rabbit Anti-Hin47 Mutant                                 antiserum against Hib in infant rat model of bacteremia                        Number of Animals                                                              cfu of Bacteria/2.5 μL Blood                                                                Av. 50   Av. 200                                                                               Av. 650 Total                                  Antibody                                                                               Av. 0   (10-100) (100-300)                                                                             (300-1,000)                                                                            Animals                                ______________________________________                                         Anti-Hin47*                                                                            3       3        2      1       9                                      Prebleed                                                                               0       4        1      4       9                                      ______________________________________                                          Groups of nine 6day old infant rats were immunized s.c. with either a          rabbit antiHin47 mutant antiserum or the corresponding prebleed serum.         Animals were challenged i.p. with 700 cfu H. influenzae strain MinnA afte      24 hours. The blood samples were taken at 20 hours after the challenge.        AntiHin47* antibody: rabbit immune serum raised against purified Hin47         mutant in CFA/IFA.                                                             Average bacteria recovery from immunized group: 100 cfu per 2.5 μL of       blood; from control group: 290 cfu per 2.5 μL of blood.               

REFERENCE LIST

1. Zangwill et al, 1993 MMWR 42:1-15.

2. Schoendorf et al, 1994 Pediatrics 93:663-8.

3. Brenner et al, 1988 Nature 334:528-530.

4. O'Hagan 1992 Clin. Pharmokinet. 22:1-10.

5. Ulmer et al, 1993 Curr. Opinion. Invest. Drugs 2:983-989.

6. Chang et al, 1978 Nature 275:617.

7. Goeddel et al 1980 Nucl. Acid. Res. 8:4057.

8. Harkness et al, 1992 J. Bacteriol. 174:2425-2430.

9. Loeb et al, 1987 Infec. Immun. 55:2612-2618.

10. Holmes and Quigley 1981. Analyt. Biochem. 114:193-197.

11. Young and Davis 1985 Gene 38:31-38.

12. Panezutti et al, 1993 Infec. Immun. 61:1867-72.

    __________________________________________________________________________     SEQUENCE LISTING                                                               (1) GENERAL INFORMATION:                                                       (iii) NUMBER OF SEQUENCES: 23                                                  (2) INFORMATION FOR SEQ ID NO:1:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 2894 base pairs                                                    (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:                                        GGATCCGTTAATACTGAAATAAATGGCACACCTTTTTCACGCATTTGGGCAAGTACAGCA60                 CTGGTTTTTGCCATTTGCATTAAAGAGAATAATGCTTCCTGCATACGAGCACCACCACTC120                GCAGAGAAACATACAAACGGACAATTCATTTCCATCGCTTTTTCAGCCGCTTTAACAAAT180                TTTGCACCAACTACAGAACCCATTGAACCGCCCATAAAAGCAAAGTTCGATGCAGCCACA240                ACAATTGGCATATCATAAAGTGTACCTGTCATAGTAATTAGCGCATCTTTCTCGCCCGTT300                TCTTTTTGTGCCGCATTGATACGATCTTTATATTTCTTTAAATCTTTAAATTTTAAAATA360                TCTTTTGGTTCTAAATCTGCCGCAATTTCTTGGCTTGAATCTTCGTCCAATAAATTTAAT420                AAACGCTCACGAGCATCAATACGCATATGATGACCACATTTCGGGCAAACATACAGATTA480                CGTTTGAGTTCTTCACTATAAAGTACTTGTTCACAAGCAGTACATTTTGTCCATACGCCT540                TCTGGCACATTGGCTTTTCGAGTGGAAGAAGAAGGACTTTTACTAAAAATTCGGTTAATC600                CAGCTCATTTTTTGACCTTTTTATTGACTAGAAAATTGCGCGTATTAGAACATAAATTTA660                TAGAATTTGCTACTTGTAAGACCGTTTTTGTACTGCTCCGATTTCCTTTTAAACAAGATA720                ATTTGCTCTCCTCTTATTGAACATTTTTTTTATTTTTTTGTCTTACTGACCACGTTATCT780                GAAATTTATTTTGGAGTATTTATGAAAAAAACACGTTTTGTACTAAATAGTATTGCACTT840                GGATTAAGTGTATTAAGCACATCATTTGTTGCTCAAGCCACTTTGCCAAGTTTTGTTTCG900                GAACAAAACAGTCTTGCACCAATGTTAGAAAAAGTACAACCTGCCGTTGTCACTCTTTCC960                GTTGAAGGAAAAGCTAAAGTAGATTCTCGTTCTCCTTTCCTAGACGATATTCCTGAAGAA1020               TTTAAATTCTTCTTTGGCGATCGTTTTGCCGAACAATTTGGTGGACGTGGAGAATCAAAG1080               CGTAACTTCCGTGGTTTAGGTTCTGGTGTCATTATTAATGCAAGCAAAGGCTATGTTTTA1140               ACCAATAATCATGTTATTGATGAAGCTGATAAAATTACCGTGCAATTACAAGATGGGCGT1200               GAATTTAAAGCAAAATTAGTGGGTAAAGATGAACTATCAGATATTGCATTAGTACAGCTT1260               GAAAAACCAAGTAATTTAACAGAAATCAAATTTGCTGATTCCGACAAATTACGCGTAGGC1320               GATTTCACTGTTGCAATCGGTAATCCATTTGGTTTAGGTCAAACTGTGACATCAGGTATT1380               GTTTCTGCATTGGGTCGTTCAACAGGTTCTGACAGTGGCACTTATGAAAACTATATTCAA1440               ACCGATGCAGCAGTAAACCGCGGTAATTCGGGTGGAGCGTTAGTAAACTTAAATGGCGAA1500               CTTATTGGAATTAATACCGCAATTATTTCTCCAAGCGGTGGCAATGCAGGAATTGCCTTT1560               GCGATTCCAAGTAATCAAGCAAGCAATTTAGTGCAACAAATTTTAGAATTTGGTCAAGTG1620               CGTCGCGGATTGCTTGGTATTAAAGGTGGCGAACTCAATGCTGATTTAGCCAAAGCCTTT1680               AATGTAAGCGCGCAACAAGGCGCATTTGTAAGTGAAGTTTTACCGAAATCTGCTGCTGAA1740               AAAGCAGGACTTAAAGCGGGCGATATTATCACGGCGATGAACGGTCAAAAAATCTCAAGT1800               TTCGCTGAAATTCGTGCAAAAATCGCAACCACTGGTGCAGGCAAAGAGATTAGCTTGACT1860               TACTTACGTGATGGCAAATCCCACGACGTTAAAATGAAATTACAAGCGGATGATAGTAGC1920               CAACTTTCCTCAAAAACTGAGTTGCCTGCATTAGATGGTGCAACATTGAAAGACTACGAT1980               GCTAAAGGCGTTAAAGGAATTGAAATCACAAAAATTCAACCTAATTCGCTGGCTGCACAA2040               CGTGGTTTAAAATCGGGCGATATTATTATTGGTATTAATCGTCAAATGATCGAAAACATT2100               CGTGAATTAAATAAAGTGCTTGAAACTGAACCGTCAGCAGTTGCACTTAATATTTTACGA2160               GGTGACAGTAATTTCTATTTATTAGTGCAATAATCTGCTTGATATATTTAAGAAAAAAGT2220               CCGATCACAATGATCGGGCTTCTTTTTATGCAGCAATCGTTCTTAACAAATCCACCACAA2280               ATTCTAACCGCACTTTGTTATCAGATAAATCTTTCATGAACTTAAATTTTAATGGGCCAT2340               CAAATCGATACACAATAGGTTCTTTTTGAATTAATTGAATAAATTTATCTGGATTCACTT2400               GTGCTTTTGCTGAAAACTCAATAAAACCGCCTTGTGTTCCTGCATCAATTCGCACAACTT2460               TCAACGGCTCAACCAACAAACGCAATTCTGCAATTTGCAGTAAATTTTTTGTTGCATCAG2520               GCAATAATCCGAATCGATCTATTAACTCAACTTTTAATTCATCTAATTCTGCTTTACTCT2580               CTGCTGCAGCAATGCGTTTATAAAAGGATAAACGCATATTCACGTCTCCTAGATAATCAT2640               CAGGCAGTAAAGCAGGCACACGCAATTCAATATCCGCTTGTTGTTGCGTCAATTCTTCTA2700               ATGATGGTTCACGCCCTTCTTTTAACGCTTTAACCGCTGCATCCAATAATTCCATATAAA2760               GCGAAAAACCGATGCTTTCAATTTGTCCACTTTGTTCGTTTCCAAGTAATTCGCCGGCAC2820               CACGAATCTCTAAATCGTGGGTTGCCAAGATAAAACCAGCCCCAAGATTATCAAGATTTT2880               CCAAGGCATCTAGA2894                                                             (2) INFORMATION FOR SEQ ID NO:2:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 463 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:                                        MetLysLysThrArgPheValLeuAsnSerIleAlaLeuGlyLeuSer                               151015                                                                         ValLeuSerThrSerPheValAlaGlnAlaThrLeuProSerPheVal                               202530                                                                         SerGluGlnAsnSerLeuAlaProMetLeuGluLysValGlnProAla                               354045                                                                         ValValThrLeuSerValGluGlyLysAlaLysValAspSerArgSer                               505560                                                                         ProPheLeuAspAspIleProGluGluPheLysPhePhePheGlyAsp                               65707580                                                                       ArgPheAlaGluGlnPheGlyGlyArgGlyGluSerLysArgAsnPhe                               859095                                                                         ArgGlyLeuGlySerGlyValIleIleAsnAlaSerLysGlyTyrVal                               100105110                                                                      LeuThrAsnAsnHisValIleAspGluAlaAspLysIleThrValGln                               115120125                                                                      LeuGlnAspGlyArgGluPheLysAlaLysLeuValGlyLysAspGlu                               130135140                                                                      LeuSerAspIleAlaLeuValGlnLeuGluLysProSerAsnLeuThr                               145150155160                                                                   GluIleLysPheAlaAspSerAspLysLeuArgValGlyAspPheThr                               165170175                                                                      ValAlaIleGlyAsnProPheGlyLeuGlyGlnThrValThrSerGly                               180185190                                                                      IleValSerAlaLeuGlyArgSerThrGlySerAspSerGlyThrTyr                               195200205                                                                      GluAsnTyrIleGlnThrAspAlaAlaValAsnArgGlyAsnSerGly                               210215220                                                                      GlyAlaLeuValAsnLeuAsnGlyGluLeuIleGlyIleAsnThrAla                               225230235240                                                                   IleIleSerProSerGlyGlyAsnAlaGlyIleAlaPheAlaIlePro                               245250255                                                                      SerAsnGlnAlaSerAsnLeuValGlnGlnIleLeuGluPheGlyGln                               260265270                                                                      ValArgArgGlyLeuLeuGlyIleLysGlyGlyGluLeuAsnAlaAsp                               275280285                                                                      LeuAlaLysAlaPheAsnValSerAlaGlnGlnGlyAlaPheValSer                               290295300                                                                      GluValLeuProLysSerAlaAlaGluLysAlaGlyLeuLysAlaGly                               305310315320                                                                   AspIleIleThrAlaMetAsnGlyGlnLysIleSerSerPheAlaGlu                               325330335                                                                      IleArgAlaLysIleAlaThrThrGlyAlaGlyLysGluIleSerLeu                               340345350                                                                      ThrTyrLeuArgAspGlyLysSerHisAspValLysMetLysLeuGln                               355360365                                                                      AlaAspAspSerSerGlnLeuSerSerLysThrGluLeuProAlaLeu                               370375380                                                                      AspGlyAlaThrLeuLysAspTyrAspAlaLysGlyValLysGlyIle                               385390395400                                                                   GluIleThrLysIleGlnProAsnSerLeuAlaAlaGlnArgGlyLeu                               405410415                                                                      LysSerGlyAspIleIleIleGlyIleAsnArgGlnMetIleGluAsn                               420425430                                                                      IleArgGluLeuAsnLysValLeuGluThrGluProSerAlaValAla                               435440445                                                                      LeuAsnIleLeuArgGlyAspSerAsnPheTyrLeuLeuValGln                                  450455460                                                                      (2) INFORMATION FOR SEQ ID NO:3:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 41 base pairs                                                      (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:                                        ATGAAAAAAACACGTTTTGTATTAAATAGTATTGCACTTGG41                                    (2) INFORMATION FOR SEQ ID NO:4:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 37 amino acids                                                     (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:                                        MetLysLysThrArgPheValLeuAsnSerIleAlaLeuGlyLeuSer                               151015                                                                         ValLeuSerThrSerPheValAlaGlnAlaThrLeuProSerPheVal                               202530                                                                         SerGluGlnAsnSer                                                                35                                                                             (2) INFORMATION FOR SEQ ID NO:5:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 472 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:                                        MetLysLysThrThrLeuAlaLeuSerArgLeuAlaLeuSerLeuSer                               151015                                                                         LeuAlaLeuSerProLeuSerAlaThrAlaAlaGluThrSerSerAla                               202530                                                                         ThrThrAlaGlnGlnMetProSerLeuAlaProMetLeuGluLysVal                               354045                                                                         MetProSerValValSerIleAsnValGluGlySerThrThrValAsn                               505560                                                                         ThrProArgMetProArgAsnPheGlnGlnPhePheGlyAspAspSer                               65707580                                                                       ProPheCysGlnGluGlySerProPheGlnSerSerProPheCysGln                               859095                                                                         GlyGlyGlnGlyGlyAsnGlyGlyGlyGlnGlnGlnLysPheMetAla                               100105110                                                                      LeuGlySerGlyValIleIleAspAlaAspLysGlyTyrValValThr                               115120125                                                                      AsnAsnHisValValAspAsnAlaThrValIleLysValGlnLeuSer                               130135140                                                                      AspGlyArgLysPheAspAlaLysMetValGlyLysAspProArgSer                               145150155160                                                                   AspIleAlaLeuIleGlnIleGlnAsnProLysAsnLeuThrAlaIle                               165170175                                                                      LysMetAlaAspSerAspAlaLeuArgValGlyAspTyrThrValGly                               180185190                                                                      IleGlyAsnProPheGlyLeuGlyGluThrValThrSerGlyIleVal                               195200205                                                                      SerAlaLeuGlyArgSerGlyLeuAsnAlaGluAsnTyrGluAsnPhe                               210215220                                                                      IleGlnThrAspAlaAlaIleAsnArgGlyAsnSerGlyGlyAlaLeu                               225230235240                                                                   ValAsnLeuAsnGlyGluLeuIleGlyIleAsnThrAlaIleLeuAla                               245250255                                                                      ProAspGlyGlyAsnIleGlyIleGlyPheAlaIleProSerAsnMet                               260265270                                                                      ValLysAsnLeuThrSerGlnMetValGluTyrGlyGlnValLysArg                               275280285                                                                      GlyGluLeuGlyIleMetGlyThrGluLeuAsnSerGluLeuAlaLys                               290295300                                                                      AlaMetLysValAspAlaGlnArgGlyAlaPheValSerGlnValLeu                               305310315320                                                                   ProAsnSerSerAlaAlaLysAlaGlyIleLysAlaGlyAspValIle                               325330335                                                                      ThrSerLeuAsnGlyLysProIleSerSerPheAlaAlaLeuArgAla                               340345350                                                                      GlnValGlyThrMetProValGlySerLysLeuThrLeuGlyLeuLeu                               355360365                                                                      ArgAspGlyLysGlnValAsnValAsnLeuGluLeuGlnGlnSerSer                               370375380                                                                      GlnAsnGlnValAspSerSerSerIlePheAsnGlyIleGluGlyAla                               385390395400                                                                   GluMetSerAsnLysGlyLysAspGlnGlyValValValAsnAsnVal                               405410415                                                                      LysThrGlyThrProAlaAlaGlnIleGlyLeuLysLysGlyAspVal                               420425430                                                                      IleIleGlyAlaAsnGlnIleAlaValLysAsnIleAlaGluIleArg                               435440445                                                                      LysValLeuAspSerLysProSerValLeuAlaLeuAsnIleGlnArg                               450455460                                                                      GlyAspArgHisLeuProValAsn                                                       465470                                                                         (2) INFORMATION FOR SEQ ID NO:6:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 475 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:                                        MetLysLysThrThrLeuAlaMetSerAlaLeuAlaLeuSerLeuGly                               151015                                                                         LeuAlaLeuSerProLeuSerAlaThrAlaAlaGluThrSerSerSer                               202530                                                                         AlaMetThrAlaGlnGlnMetProSerLeuAlaProMetLeuGluLys                               354045                                                                         ValMetProSerValValSerIleAsnValGluGlySerThrThrVal                               505560                                                                         AsnThrProArgMetProArgAsnPheGlnGlnPhePheGlyAspAsp                               65707580                                                                       SerProPheCysGlnAspGlySerProPheGlnAsnSerProPheCys                               859095                                                                         GlnGlyGlyGlyAsnGlyGlyAsnGlyGlyGlnGlnGlnLysPheMet                               100105110                                                                      AlaLeuGlySerGlyValIleIleAspAlaAspLysGlyTyrValVal                               115120125                                                                      ThrAsnAsnHisValValAspAsnAlaSerValIleLysValGlnLeu                               130135140                                                                      SerAspGlyArgLysPheAspAlaLysValValGlyLysAspProArg                               145150155160                                                                   SerAspIleAlaLeuIleGlnIleGlnAsnProLysAsnLeuThrAla                               165170175                                                                      IleLysLeuAlaAspSerAspAlaLeuArgValGlyAspTyrThrVal                               180185190                                                                      AlaIleGlyAsnProPheGlyLeuGlyGluThrValThrSerGlyIle                               195200205                                                                      ValSerAlaLeuGlyArgSerGlyLeuAsnValGluAsnTyrGluAsn                               210215220                                                                      PheIleGlnThrAspAlaAlaIleAsnArgGlyAsnSerGlyGlyAla                               225230235240                                                                   LeuValAsnLeuAsnGlyGluLeuIleGlyIleAsnThrAlaIleLeu                               245250255                                                                      AlaProAspGlyGlyAsnIleGlyIleGlyPheAlaIleProSerAsn                               260265270                                                                      MetValLysAsnLeuThrSerGlnMetValGluTyrGlyGlnValArg                               275280285                                                                      ArgGlyGluLeuGlyIleMetGlyThrGluLeuAsnSerGluLeuAla                               290295300                                                                      LysAlaMetLysValAspAlaGlnArgGlyAlaPheValSerGlnVal                               305310315320                                                                   MetProAsnSerSerAlaAlaLysAlaGlyIleLysAlaGlyAspVal                               325330335                                                                      IleThrSerLeuAsnGlyLysProIleSerSerPheAlaAlaLeuArg                               340345350                                                                      AlaGlnValGlyThrMetProValGlySerLysIleSerLeuGlyLeu                               355360365                                                                      LeuArgGluGlyLysAlaIleThrValAsnLeuGluLeuGlnGlnSer                               370375380                                                                      SerGlnSerGlnValAspSerSerThrIlePheSerGlyIleGluGly                               385390395400                                                                   AlaGluMetSerAsnLysGlyGlnAspLysGlyValValValSerSer                               405410415                                                                      ValLysAlaAsnSerProAlaAlaGlnIleGlyLeuLysLysGlyAsp                               420425430                                                                      ValIleIleGlyAlaAsnGlnIleProValLysAsnIleAlaGluIle                               435440445                                                                      ArgLysIleLeuAspSerLysProSerValLeuAlaLeuAsnIleGln                               450455460                                                                      ArgGlyAspSerSerIleTyrLeuLeuMetGln                                              465470475                                                                      (2) INFORMATION FOR SEQ ID NO:7:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 228 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:                                        IleValGlyGlyTyrLysCysGluLysAsnSerGlnProTrpGlnVal                               151015                                                                         AlaValIleAsnGluTyrLeuCysGlyGlyValLeuIleAspProSer                               202530                                                                         TrpValIleThrAlaAlaHisCysTyrSerAsnAsnTyrGlnValLeu                               354045                                                                         LeuGlyArgAsnAsnLeuPheLysAspGluProPheAlaGlnArgArg                               505560                                                                         LeuValProGlnSerPheArgHisProAspTyrIleProLeuIlePro                               65707580                                                                       ValHisAspHisSerAsnAspLeuMetLeuLeuHisLeuSerGluPro                               859095                                                                         AlaAspIleThrGlyGlyValLysValIleAspLeuProThrLysGlu                               100105110                                                                      ProLysValGlySerThrCysLeuAlaSerGlyTrpGlySerThrAsn                               115120125                                                                      ProSerGluMetValValSerHisAspLeuGlnCysValAsnIleHis                               130135140                                                                      LeuLeuSerAsnGluLysCysIleGluThrTyrLysAspAsnValThr                               145150155160                                                                   AspValMetLeuCysAlaGlyGluMetGluGlyGlyLysAspThrCys                               165170175                                                                      AlaGlyAspSerGlyGlyProLeuIleCysAspGlyValLeuGlnGly                               180185190                                                                      IleThrSerGlyGlyAlaThrProCysAlaLysProLysThrProAla                               195200205                                                                      IleTyrAlaLysLeuIleLysPheThrSerTrpIleLysLysValMet                               210215220                                                                      LysGluAsnPro                                                                   225                                                                            (2) INFORMATION FOR SEQ ID NO:8:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 232 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:                                        IleIleGlyGlyArgGluCysGluLysAsnSerHisProTrpGlnVal                               151015                                                                         AlaIleTyrHisTyrSerSerPheGlnCysGlyGlyValLeuValAsn                               202530                                                                         ProLysTrpValLeuThrAlaAlaHisCysLysAsnAspAsnTyrGlu                               354045                                                                         ValTrpLeuGlyArgHisAsnLeuPheGluAsnGluAsnThrAlaGln                               505560                                                                         PhePheGlyValThrAlaAspPheProHisProGlyPheAsnLeuSer                               65707580                                                                       AlaAspGlyLysAspTyrSerHisAspLeuMetLeuLeuArgLeuGln                               859095                                                                         SerProAlaLysIleThrAspAlaValLysValLeuGluLeuProThr                               100105110                                                                      GlnGluProGluLeuGlySerThrCysGluAlaSerGlyTrpGlySer                               115120125                                                                      IleGluProGlyProAspAspPheGluPheProAspGluIleGlnCys                               130135140                                                                      ValGlnLeuThrLeuLeuGlnAsnThrPheCysAlaAspAlaHisPro                               145150155160                                                                   AspLysValThrGluSerMetLeuCysAlaGlyTyrLeuProGlyGly                               165170175                                                                      LysAspThrCysMetGlyAspSerGlyGlyProLeuIleCysAsnGly                               180185190                                                                      MetTrpGlnGlyIleThrSerTrpGlyHisThrProCysGlySerAla                               195200205                                                                      AsnLysProSerIleTyrThrLysLeuIlePheTyrLeuAspTrpIle                               210215220                                                                      AspAspThrIleThrGluAsnPro                                                       225230                                                                         (2) INFORMATION FOR SEQ ID NO:9:                                               (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 223 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:                                        IleValGlyGlyTyrThrCysGlyAlaAsnThrValProTyrGlnVal                               151015                                                                         SerLeuAsnSerGlyTyrHisPheCysGlyGlySerLeuIleAsnSer                               202530                                                                         GlnTrpValValSerAlaAlaHisCysTyrLysSerGlyIleGlnVal                               354045                                                                         ArgLeuGlyGluAspAsnIleAsnValValGluGlyAsnGluGlnPhe                               505560                                                                         IleSerAlaSerLysSerIleValHisProSerTyrAsnSerAsnThr                               65707580                                                                       LeuAsnAsnAspIleMetLeuIleLysLeuLysSerAlaAlaSerLeu                               859095                                                                         AsnSerArgValAlaSerIleSerLeuProThrSerCysAlaSerAla                               100105110                                                                      GlyThrGlnCysLeuIleSerGlyTrpGlyAsnThrLysSerSerGly                               115120125                                                                      ThrSerTyrProAspValLeuLysCysLeuLysAlaProIleLeuSer                               130135140                                                                      AspSerSerCysLysSerAlaTyrProGlyGlnIleThrSerAsnMet                               145150155160                                                                   PheCysAlaGlyTyrLeuGluGlyGlyLysAspSerCysGlnGlyAsp                               165170175                                                                      SerGlyGlyProValValCysSerGlyLysLeuGlnGlyIleValSer                               180185190                                                                      TrpGlySerGlyCysAlaGlnLysAsnLysProGlyValTyrThrLys                               195200205                                                                      ValCysAsnTyrValSerTrpIleLysGlnThrIleAlaSerAsn                                  210215220                                                                      (2) INFORMATION FOR SEQ ID NO:10:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 228 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:                                       IleValAsnGlyGluGluAlaValProGlySerTrpProTrpGlnVal                               151015                                                                         SerLeuGlnAspLysThrGlyPheHisPheCysGlyGlySerLeuIle                               202530                                                                         AsnGluAsnTrpValValThrAlaAlaHisCysGlyValThrThrSer                               354045                                                                         AspValValValAlaGlyGluPheAspGlnGlySerSerSerGluLys                               505560                                                                         IleGlnLysLeuLysIleAlaLysValPheLysAsnSerLysTyrAsn                               65707580                                                                       SerLeuThrIleAsnAsnAspIleThrLeuLeuLysLeuSerThrAla                               859095                                                                         AlaSerPheSerGlnThrValSerAlaValCysLeuProSerAlaSer                               100105110                                                                      AspAspPheAlaAlaGlyThrThrCysValThrThrGlyTrpGlyLeu                               115120125                                                                      ThrArgTyrAlaAsnThrProAspArgLeuGlnGlnAlaSerLeuPro                               130135140                                                                      LeuLeuSerAsnThrAsnCysLysLysTyrTrpGlyThrLysIleLys                               145150155160                                                                   AspAlaMetIleCysAlaGlyAlaSerGlyValSerSerCysMetGly                               165170175                                                                      AspSerGlyGlyProLeuValCysLysLysAsnGlyAlaTrpThrLeu                               180185190                                                                      ValGlyIleValSerTrpGlySerSerThrCysSerThrSerThrPro                               195200205                                                                      GlyValTyrAlaArgValThrAlaLeuValAsnTrpValGlnGlnThr                               210215220                                                                      LeuAlaAlaAsn                                                                   225                                                                            (2) INFORMATION FOR SEQ ID NO:11:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 240 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:                                       ValValGlyGlyThrGluAlaGlnArgAsnSerTrpProSerGlnIle                               151015                                                                         SerLeuGlnTyrArgSerGlySerSerTrpAlaHisThrCysGlyGly                               202530                                                                         ThrLeuIleArgGlnAsnTrpValMetThrAlaAlaHisCysValAsp                               354045                                                                         ArgGluLeuThrPheArgValValValGlyGluHisAsnLeuAsnGln                               505560                                                                         AsnAsnGlyThrGluGlnTyrValGlyValGlnLysIleValValHis                               65707580                                                                       ProTyrTrpAsnThrAspAspValAlaAlaGlyTyrAspIleAlaLeu                               859095                                                                         LeuArgLeuAlaGlnSerValThrLeuAsnSerTyrValGlnLeuGly                               100105110                                                                      ValLeuProArgAlaGlyThrIleLeuAlaAsnAsnSerProCysTyr                               115120125                                                                      IleThrGlyTrpGlyLeuThrArgThrAsnGlyGlnLeuAlaGlnThr                               130135140                                                                      LeuGlnGlnAlaTyrLeuProThrValAspTyrAlaIleCysSerSer                               145150155160                                                                   SerSerTyrTrpGlySerThrValLysAsnSerMetValCysAlaGly                               165170175                                                                      GlyAspGlyValArgSerGlyCysGlnGlyAspSerGlyGlyProLeu                               180185190                                                                      HisCysLeuValAsnGlyGlnTyrAlaValHisGlyValThrSerPhe                               195200205                                                                      ValSerArgLeuGlyCysAsnValThrArgLysProThrValPheThr                               210215220                                                                      ArgValSerAlaTyrIleSerTrpIleAsnAsnValIleAlaSerAsn                               225230235240                                                                   (2) INFORMATION FOR SEQ ID NO:12:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 224 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:                                       IleIleGlyGlyValGluSerIleProHisSerArgProTyrMetAla                               151015                                                                         HisLeuAspIleValThrGluLysGlyLeuArgValIleCysGlyGly                               202530                                                                         PheLeuIleSerArgGlnPheValLeuThrAlaAlaHisCysLysGly                               354045                                                                         ArgGluIleThrValIleLeuGlyAlaHisAspValArgLysArgGlu                               505560                                                                         SerThrGlnGlnLysIleLysValGluLysGlnIleIleHisGluSer                               65707580                                                                       TyrAsnSerValProAsnLeuHisAspIleMetLeuLeuLysLeuGlu                               859095                                                                         LysLysValGluLeuThrProAlaValAsnValValProLeuProSer                               100105110                                                                      ProSerAspPheIleHisProGlyAlaMetCysTrpAlaAlaGlyTrp                               115120125                                                                      GlyLysThrGlyValArgAspProThrSerTyrThrLeuArgGluVal                               130135140                                                                      GluLeuArgIleMetAspGluLysAlaCysValAspTyrArgTyrTyr                               145150155160                                                                   GluTyrLysPheGlnValCysValGlySerProThrThrLeuArgAla                               165170175                                                                      AlaPheMetGlyAspSerGlyGlyProLeuLeuCysAlaGlyValAla                               180185190                                                                      HisGlyIleValSerTyrGlyHisProAspAlaLysProProAlaIle                               195200205                                                                      PheThrArgValSerThrTyrValProTrpIleAsnAlaValIleAsn                               210215220                                                                      (2) INFORMATION FOR SEQ ID NO:13:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 223 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:                                       ValValGlyGlyThrArgAlaAlaGlnGlyGluPheProPheMetVal                               151015                                                                         ArgLeuSerMetGlyCysGlyGlyAlaLeuTyrAlaGlnAspIleVal                               202530                                                                         LeuThrAlaAlaHisCysValSerGlySerGlyAsnAsnThrSerIle                               354045                                                                         ThrAlaThrGlyGlyValValAspLeuGlnSerGlyAlaAlaValLys                               505560                                                                         ValArgSerThrLysValLeuGlnAlaProGlyTyrAsnGlyThrGly                               65707580                                                                       LysAspTrpAlaLeuIleLysLeuAlaGlnProIleAsnGlnProThr                               859095                                                                         LeuLysIleAlaThrThrThrAlaTyrAsnGlnGlyThrPheThrVal                               100105110                                                                      AlaGlyTrpGlyAlaAsnArgGluGlyGlySerGlnGlnArgTyrLeu                               115120125                                                                      LeuLysAlaAsnValProPheValSerAspAlaAlaCysArgSerAla                               130135140                                                                      TyrGlyAsnGluLeuValAlaAsnGluGluIleCysAlaGlyTyrPro                               145150155160                                                                   AspThrGlyGlyValAspThrCysGlnGlyAspSerGlyGlyProMet                               165170175                                                                      PheArgLysAspAsnAlaAspGluTrpIleGlnValGlyIleValSer                               180185190                                                                      TrpGlyTyrGlyCysAlaArgProGlyTyrProGlyValTyrThrGlu                               195200205                                                                      ValSerThrPheAlaSerAlaIleAlaSerAlaAlaArgThrLeu                                  210215220                                                                      (2) INFORMATION FOR SEQ ID NO:14:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 185 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:                                       IleSerGlyGlyAspAlaIleTyrSerSerThrGlyArgCysSerLeu                               151015                                                                         GlyPheAsnValArgSerGlySerThrTyrTyrPheLeuThrAlaGly                               202530                                                                         HisCysThrAspGlyAlaThrThrTrpTrpAlaAsnSerAlaArgThr                               354045                                                                         ThrValLeuGlyThrThrSerGlySerSerPheProAsnAsnAspTyr                               505560                                                                         GlyIleValArgTyrThrAsnThrThrIleProLysAspGlyThrVal                               65707580                                                                       GlyGlyGlnAspIleThrSerAlaAlaAsnAlaThrValGlyMetAla                               859095                                                                         ValThrArgArgGlySerThrThrGlyThrHisSerGlySerValThr                               100105110                                                                      AlaLeuAsnAlaThrValAsnTyrGlyGlyGlyAspValValTyrGly                               115120125                                                                      MetIleArgThrAsnValCysAlaGluProGlyAspSerGlyGlyPro                               130135140                                                                      LeuTyrSerGlyThrArgAlaIleGlyLeuThrSerGlyGlySerGly                               145150155160                                                                   AsnCysSerSerGlyGlyThrThrPhePheGlnProValThrGluAla                               165170175                                                                      LeuValAlaTyrGlyValSerValTyr                                                    180185                                                                         (2) INFORMATION FOR SEQ ID NO:15:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 181 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:                                       IleAlaGlyGlyGluAlaIleThrThrGlyGlySerArgCysSerLeu                               151015                                                                         GlyPheAsnValSerValAsnGlyValAlaHisAlaLeuThrAlaGly                               202530                                                                         HisCysThrAsnIleSerAlaSerTrpSerIleGlyThrArgThrGly                               354045                                                                         ThrSerPheProAsnAsnAspTyrGlyIleIleArgHisSerAsnPro                               505560                                                                         AlaAlaAlaAspGlyArgValTyrLeuTyrAsnGlySerTyrGlnAsp                               65707580                                                                       IleThrThrAlaGlyAsnAlaPheValGlyGlnAlaValGlnArgSer                               859095                                                                         GlySerThrThrGlyLeuArgSerGlySerValThrGlyLeuAsnAla                               100105110                                                                      ThrValAsnTyrGlySerSerGlyIleValTyrGlyMetIleGlnThr                               115120125                                                                      AsnValCysAlaGlnProGlyAspSerGlyGlySerLeuPheAlaGly                               130135140                                                                      SerThrAlaLeuGlyLeuThrSerGlyGlySerGlyAsnCysArgThr                               145150155160                                                                   GlyGlyThrThrPheTyrGlnProValThrGluAlaLeuSerAlaTyr                               165170175                                                                      GlyAlaThrValLeu                                                                180                                                                            (2) INFORMATION FOR SEQ ID NO:16:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 198 amino acids                                                    (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16:                                       AlaAsnIleValGlyGlyIleGluTyrSerIleAsnAsnAlaSerLeu                               151015                                                                         CysSerValGlyPheSerValThrArgGlyAlaThrLysGlyPheVal                               202530                                                                         ThrAlaGlyHisCysGlyThrValAsnAlaThrAlaArgIleGlyGly                               354045                                                                         AlaValValGlyThrPheAlaAlaArgValPheProGlyAsnAspArg                               505560                                                                         AlaTrpValSerLeuThrSerAlaGlnThrLeuLeuProArgValAla                               65707580                                                                       AsnGlySerSerPheValThrValArgGlySerThrGluAlaAlaVal                               859095                                                                         GlyAlaAlaValCysArgSerGlyArgThrThrGlyTyrGlnCysGly                               100105110                                                                      ThrIleThrAlaLysHisValThrAlaAsnTyrAlaGluGlyAlaVal                               115120125                                                                      ArgGlyLeuThrGlnGlyAsnAlaCysMetGlyArgGlyAspSerGly                               130135140                                                                      GlySerTrpIleThrSerAlaGlyGlnAlaGlnGlyValMetSerGly                               145150155160                                                                   GlyAsnValGlnSerAsnGlyAsnAsnCysGlyIleProAlaSerGln                               165170175                                                                      ArgSerSerLeuPheGluArgLeuGlnProIleLeuSerGlnTyrGly                               180185190                                                                      LeuSerLeuValThrGly                                                             195                                                                            (2) INFORMATION FOR SEQ ID NO:17:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 7 amino acids                                                      (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:                                       GlyAsnSerGlyGlyAlaLeu                                                          15                                                                             (2) INFORMATION FOR SEQ ID NO:18:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 7 amino acids                                                      (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18:                                       GlyAspSerGlyGlyProLys                                                          15                                                                             (2) INFORMATION FOR SEQ ID NO:19:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 14 amino acids                                                     (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19:                                       MetLysLysThrArgPheValLeuAsnSerIleAlaLeuGly                                     1510                                                                           (2) INFORMATION FOR SEQ ID NO:20:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 22 base pairs                                                      (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20:                                       CGCTCCACCAGCATTACCGCGG22                                                       (2) INFORMATION FOR SEQ ID NO:21:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 21 base pairs                                                      (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21:                                       ATCAATAACAGCATTATTGGT21                                                        (2) INFORMATION FOR SEQ ID NO:22:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 21 base pairs                                                      (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22:                                       TAATGCAATTGCTGATAGTTC21                                                        (2) INFORMATION FOR SEQ ID NO:23:                                              (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 11 amino acids                                                     (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                           (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23:                                       LysPhePhePheGlyAspArgPheAlaGluGln                                              1510                                                                           __________________________________________________________________________ 

What we claim is:
 1. A method of determining the presence of antibodies specifically reactive with Hin47 protein in a sample, comprising the steps of:(a) contacting the sample with an isolated and purified analog of Haemophilus influenzae Hin47 protein having a decreased protease activity which is less than about 10% of that of natural Hin47 protein, wherein at least one amino acid of the natural Hin47 protein contributing to protease activity and which is selected from the group consisting of amino acids 91, 121 and 195 to 201 of natural Hin47 protein has been deleted or replaced by a different amino acid to provide said reduced protease activity and which has substantially the same immunogenic properties as natural Hin47 protein to produce complexes comprising said analog and any antibodies present in the sample specifically reactive therewith; and (b) determining production of the complexes.
 2. A method of determining the presence of Hin 1 in a sample comprising the steps of:(a) immunizing a subject with an immunogenic composition, comprising an immuno-effective amount of an isolated and purified analog of Haemophilus influenzae Hin47 protein having a decreased protease activity which is less than about 10% of that of natural Hin47 protein, wherein at least one amino acid of the natural Hin47 protein contributing to protease activity and which is selected from the group consisting of amino acids 91, 121 and 195 to 201 of natural Hin47 protein has been deleted or replaced by a different amino acid to provide said reduced protease activity and which has substantially the same immunogenic properties as natural Hin47 or an immunogenic composition, comprising an immuno-effective amount of an isolated and purified nucleic acid molecule comprising a mutant Haemophilus influenzae hin47 gene coding an analog of Haemophilus influenzae Hin47 protein having a decreased protease activity which is less than about 10% of that of natural Hin47 protein, wherein at least one codon of a wild-type hin47 gene encoding an amino acid selected from the group consisting of amino acids 91, 121 and 195 to 201, has been deleted or replaced by a codon encoding a different amino acid to provide the reduced protease activity to produce antibodies specific for Hin47 protein; (b) contacting the sample with the antibodies to produce complexes comprising any Hin47 protein present in the sample and said Hin47 protein specific antibodies; and (c) determining production of the complexes.
 3. A diagnostic kit for determining the presence of antibodies in a sample specifically reactive with Hin47 protein, comprising:(a) an isolated and purified analog of Haemophilus influenzae Hin47 protein having a decreased protease activity which is less than about 10% of that of natural Hin47 protein, wherein at least one amino acid of the natural Hin47 protein contributing to protease activity and which is selected from the group consisting of amino acids 91, 121 and 195 to 201 of natural Hin47 protein has been deleted or replaced by a different amino acid to provide said reduced protease activity and has substantially the same immunogenic properties as natural Hin47 protein; (b) means for contacting the analog with the sample to produce complexes comprising the analog and any said antibodies produced present in the sample; and (c) means for determining the production of the complexes. 